Department of Biochemistry, University of Alberta, Edmonton, Alberta T6G 2H7, Canada and Department of Oncology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
Nucleic Acids Res. 2014 Apr;42(8):5234-44. doi: 10.1093/nar/gku133. Epub 2014 Feb 11.
While functional mature microRNAs (miRNAs) are small ∼22 base oligonucleotides that target specific mRNAs, miRNAs are initially expressed as long transcripts (pri-miRNAs) that undergo sequential processing to yield the mature miRNAs. We have previously reported that the pri-miR-17∼92 cluster adopts a compact globular folded structure that internalizes a 3' core domain resulting in reduced miRNA maturation and subsequent mRNA targeting. Using a site-specific photo-cross-linker we have identified a tertiary contact within the 3' core domain of the pri-miRNA between a non-miRNA stem-loop and the pre-miR-19b hairpin. This tertiary contact is involved in the formation of the compact globular fold of the cluster while its disruption enhances miR-92a expression and mRNA targeting. We propose that this tertiary contact serves as a molecular scaffold to restrict expression of the proposed antiangiogenic miR-92a, allowing for the overall pro-angiogenic effect of miR-17∼92 expression.
功能成熟的 microRNAs(miRNAs)是靶向特定 mRNAs 的小约 22 个碱基的寡核苷酸,但 miRNA 最初是作为长转录本(pri-miRNAs)表达的,这些长转录本经过连续加工生成成熟的 miRNAs。我们之前曾报道过,pri-miR-17∼92 簇采用紧凑的球形折叠结构,内部包含一个 3'核心结构域,导致 miRNA 成熟减少,并随后靶向 mRNA。我们使用一种位点特异性光交联剂,在 pri-miRNA 的 3'核心结构域内鉴定到非 miRNA 茎环和 pre-miR-19b 发夹之间的三级接触。这种三级接触参与簇的紧凑球形折叠的形成,而其破坏增强了 miR-92a 的表达和 mRNA 靶向。我们提出,这种三级接触充当分子支架,限制拟血管生成 miR-92a 的表达,从而允许 miR-17∼92 表达的整体促血管生成作用。